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| | Fmoc-L-Pro(4-NHPoc)-OH (2S,4S) Basic information |
| Product Name: | Fmoc-L-Pro(4-NHPoc)-OH (2S,4S) | | Synonyms: | Fmoc-L-Pro(4-NHPoc)-OH (2S,4S);1,2-Pyrrolidinedicarboxylic acid, 4-[[(2-propyn-1-yloxy)carbonyl]amino]-, 1-(9H-fluoren-9-ylmethyl) ester, (2R,4R)-rel-;(2S,4S)-Fmoc-L-Pro(4-NHPoc)-OH | | CAS: | 2451202-17-6 | | MF: | C24H22N2O6 | | MW: | 434.44 | | EINECS: | | | Product Categories: | | | Mol File: | 2451202-17-6.mol |  |
| | Fmoc-L-Pro(4-NHPoc)-OH (2S,4S) Chemical Properties |
| Boiling point | 661.5±55.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | pka | 3.74±0.40(Predicted) |
| | Fmoc-L-Pro(4-NHPoc)-OH (2S,4S) Usage And Synthesis |
| Uses | (2S,4S)-Fmoc-L-Pro(4-NHPoc)-OH is a click chemistry reagent containing an azide group. | | References | [1] Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789. DOI:10.1080/17460441.2019.1614910 |
| | Fmoc-L-Pro(4-NHPoc)-OH (2S,4S) Preparation Products And Raw materials |
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